---
title: 'Clinical Trial Associate at PathAI'
canonical: 'https://feeny.ai/job/clinical-trial-associate-pathai-boston-40ze8teancve'
type: 'job'
last_seen: '2026-10-15'
---

# Clinical Trial Associate at PathAI

- **Company:** PathAI
- **Location:** Boston, MA
- **Work type:** remote
- **Posted:** 2026-10-02
- **Last confirmed live:** 2026-10-15
- **Apply:** https://www.pathai.com/careers/8863668002?gh_jid=8863668002

## Job description

## Who We Are

PathAI's mission is to improve patient outcomes with AI-powered pathology. We are transforming traditional pathology methods into powerful, new technologies. These innovations in pathology can help accelerate drug development, improve confidence in the accuracy of diagnosis, and get life-saving therapies to patients more quickly. At PathAI, you'll work with a diverse and talented team of people, who are dedicated to solving complex problems and making a huge impact.

The Opportunity

The Clinical Trial Associate (CTA), Clinical Development Services will play a vital role in the Clinical Operations team. Through responsibilities like monitoring of clinical trial lab services, engaging with clinical investigator sites and supporting the primary CTM, this role will ensure successful completion of clinical studies with a lab services component.

- Study and Activity Monitoring:
- Bring a strong understanding of GCP, ICH, and knowledge of regulatory requirements in support of successful clinical trials.
- Adhere to the Code of Federal Regulations (Title 21) and guidelines set up by the International Committee for Harmonization (ICH) for good clinical practices.
- Oversee and manage the timely closure of queries issued to clinical trial investigator sites and/or other designated parties.
- Work with the CTM to proactively identify trends and provide feedback to internal departments and/or clients on performance of both the Investigator and the PathAI BioPharma Laboratory to ensure timely service delivery.  Examples may include:
- Monitor the performance of both the Investigator(s) and/or the Laboratory as applicable
- Monitor study specific and/or Sponsor requested requirements.
- Oversee and/or monitor queries, pending results, testing TATs, etc.
- Collaborate with data management to ensure resolution of data discrepancies at all stages of the study.
- Assist with the organization and tracking of storage specimens: receipt, retrieval, and shipping as applicable.
- Coordinate with external vendors and Sponsors to ensure delivery of laboratory kits and test results to sites.
- Provide Support to CTM:
- Perform generic, routine study duties and tasks that are applicable across assigned clinical trials, including but not limited to:  receipt of site lists, drafting of site facing laboratory manuals, managing laboratory kits orders, and monitoring the day-to-day trial operations (i.e., specimen management reports, case assignments on the PathAI AISight CT Platform, monitoring pending lab analysis, etc.).
- Support the CTM for routine administrative tasks of the clinical trial (e.g., action item tracking, meeting minutes, process mapping, etc.).
- Act as a backup support for the CTM during their times of absence, including leading client communication and study management activities.
- Proactive lines of communication:
- Interact with other functional areas and/or vendors to resolve problems, enhance processes, and service delivery.
- Liaise with other departments and support services (e.g., Laboratory, Engineering, etc) to expedite testing of patient’s laboratory specimens and/or provision of kits.
- Coordinate information and communications for designated projects at the site level, including identification and escalation of discrepancies as needed.
- Assist with the development of meeting or training materials where applicable.
- Project Documentation and Deliverables:
- Assist in reviewing study start up project deliverable schedule, milestones and required tasks
- Support maintenance of project documentation files.
- Oversee and/or lead Project Close-out procedures as required.
- Assist with the development of meeting or training materials where applicable
- Perform other administrative or process-related duties as needed to support the success of the trial.

Who You Are: (Required)

- You have 3+ years of clinical research experience in medical device and/or drug development clinical trials and a BS or BA in a relevant scientific discipline.
- You have good organizational skills, attention to details, and ability to multitask.

Preferred:

- You have experience in digital pathology, radiology or other imaging technology-based clinical trials is highly preferred.
- You have Project Management Certification is a plus.

This position is based in Boston or Remote Relocation benefits are not available for this position.

The expected salary range for this position based on the primary location Boston, MA is $63,750 - $97,750.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.

PathAI is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

## About PathAI

## Core Business
- **Primary industry**: Healthcare AI / Digital Pathology / Precision Medicine
- **Target customers**: Biopharma companies (top 15 leverage their technology), anatomic pathology laboratories (academic medical centers, reference labs, health systems), and clinical research organizations.
- **Mission**: To improve patient outcomes with AI-powered pathology through more accurate diagnosis, matching patients with effective treatments, and accelerating life-saving drug approvals.

## Products & Services
- **AISight®**: A cloud-native, open platform enterprise digital pathology workflow solution for case management, image management, and AI applications. Received FDA 510(k) clearance for primary diagnosis, including a Predetermined Change Control Plan (PCCP). Also CE marked.
- **AI Algorithms**: Over 20 AI products launched (e.g., PathExplore, AIM-MASH AI Assist for NASH, PathAssist Derm – Breakthrough Device Designation). Trained on 32.5+ million annotations from a network of 450+ pathologists.
- **Precision Pathology Network (PPN)**: First global network of digital anatomic pathology laboratories launched in 2025.
- **Biopharma Lab Services**: CAP/CLIA-certified GCLP histopathology lab in Memphis supporting end-to-end clinical trials.

## Market Standing
- **Valuation**: Not publicly disclosed (private company; pending acquisition by Roche – definitive merger agreement announced April 7, 2026).
- **Key Metric**: Total funding not specified in sources, but notable milestones include FDA clearances, partnerships, and expansion of AI products.
- **Notable Investors/Partners**: Quest Diagnostics (strategic partnership, including sale of PathAI Diagnostics in 2024), Labcorp (expanded nationwide deployment of AISight), MedStar Health, and Roche (acquiring entity).
- **Growth Signals**: FDA clearance for AISight Dx with PCCP (2025); Breakthrough Device Designation for PathAssist Derm (2026); EMA and FDA qualification of AIM-MASH AI Assist as a Drug Development Tool (2025); launch of Precision Pathology Network (2025); Labcorp collaboration expansion (2026); top 15 biopharma companies as clients.

## Competitive Advantages
- **Data Moat**: 32.5+ million annotations from a proprietary network of 450+ board-certified pathologists and a vast library of archived tissue data.
- **Regulatory Leadership**: First digital pathology platform with FDA clearance including a PCCP, enabling iterative AI improvements without new submissions.
- **End-to-End Solutions**: From AI algorithms and digital pathology platform to wet lab services and clinical trial support – a comprehensive precision pathology offering.
- **Established Partnerships**: Deep relationships with major diagnostics companies (Quest, Labcorp) and biopharma leaders.

## Strategic Focus
- **Expanding AI Diagnostics**: Scaling FDA-cleared AISight Dx platform and AI algorithms across reference labs and health systems.
- **Precision Medicine**: Driving biomarker discovery and drug development tools (e.g., AIM-MASH AI Assist) to match patients with effective therapies.
- **Global Network**: Growing the Precision Pathology Network to standardize digital pathology worldwide.
- **Integration with Roche**: Post-acquisition, likely to accelerate global reach and R&D investment (deal announced April 2026).

## Why Work Here
- **Culture**: Values include patient first, accountability, team (One PathAI), humility, and being all in. Described as passionate about solving big challenges in healthcare.
- **Work Model**: Hybrid (Boston, Memphis, NYC) and remote-friendly roles available. Boston HQ in Fenway with amenities (snacks, game room, roof deck). Memphis lab office near downtown. NYC co-working space in Union Square.
- **Benefits**: Comprehensive health plans, parental leave, wellness benefits, 401(k) program, paid time off and holidays.
- **Recognition**: Named Best Places to Work in Boston (2022, 2023) and Great Place to Work Certified (2022-2023).
- **Team**: 650 total employees (as of BuiltIn data), with roles in engineering, science, and operations. Open positions listed on Greenhouse.

## Sources
1. [PathAI Official Website](https://www.pathai.com/)
2. [PathAI About – History & Leadership](https://www.pathai.com/about-us)
3. [PathAI Careers Page](https://www.pathai.com/careers)
4. [Built In – PathAI Careers, Perks & Culture](https://builtin.com/company/pathai)
5. [Crunchbase – PathAI Profile](https://www.crunchbase.com/organization/pathai)

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